gudid
Primary ID: BF16160-C2
BIO-FEATHER (UDI BF16160-C2)
Manufactured by MEDAX SRL UNIPERSONALE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BIO-FEATHER - Primary ID BF16160-C2
Device Regulatory Overview
The BIO-FEATHER (Model/Catalog Number: BF16160-C2) is a medical device manufactured by MEDAX SRL UNIPERSONALE. This product is indexed under FDA Product Code / Category Classification KNW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BF16160-C2
- Product Code / EMDN
- KNW
- Device Name
- Semi-automatic disposable biopsy system with adjustable penetration depth 16G X 160 MM
- Database Sync Date
- 2026-08-09 09:04:29
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of BIO-FEATHER?
The registered manufacturer of record for BIO-FEATHER is MEDAX SRL UNIPERSONALE.
What is the Primary UDI-DI identifier for BIO-FEATHER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BF16160-C2.
What classification code is assigned to this device?
This device is registered under product classification code KNW.
Similar Classification Devices (KNW)
Other Devices by MEDAX SRL UNIPERSONALE
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